Zobrazeno 1 - 10 of 58 pro vyhledávání: '"E. Werder"'
1
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2
No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardation
Autor: D, Kotzot, I W, Lurie, K, Méhes, E, Werder, A, Schinzel
Publikováno v: Clinical genetics. 58(3)
Intrauterine growth retardation (IUGR) is defined as length and/or weight below the 10th percentile. Etiology and, consequently, long-term outcome are extremely heterogeneous with chromosomal abnormalities found in up to 7%. Recently, uniparental dis
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::83085744420c022e2176b8bf972cdaee
https://pubmed.ncbi.nlm.nih.gov/11076039
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3
[Chronic giardiasis with intestinal dwarfism and delayed puberty in immunoglobulin deficiency syndrome: complete catch-up growth after therapy]
Autor: D, Herzog, B, Hammer, J, Neuweiler, E, Werder
Publikováno v: Schweizerische medizinische Wochenschrift. 128(16)
A 10-year-old, previously healthy Swiss boy suffered from repeated episodes of watery diarrhea for some months following a summer camp holiday. No etiology was found, and except for symptomatic treatment no other therapy was necessary. Five years lat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6f60d347a4ca6f08f53ebbf12fff4a53
https://pubmed.ncbi.nlm.nih.gov/9611305
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4
An inherited mutation associated with functional deficiency of the alpha-subunit of the guanine nucleotide-binding protein Gs in pseudo- and pseudopseudohypoparathyroidism
Autor: J A, Fischer, F, Egert, E, Werder, W, Born
Publikováno v: The Journal of clinical endocrinology and metabolism. 83(3)
Pseudohypoparathyroidism type Ia (PSP) is a disorder characterized by Albright's osteodystrophy, secondary hyperparathyroidism, lowered Gs activity, and resistance of the urinary cAMP excretion to exogenous PTH. The patients had raised basal serum le
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5728415a6a626affed6c588a0a288403
https://pubmed.ncbi.nlm.nih.gov/9506752
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5
[Transitory neonatal hypothyroidism caused by transplacental transfer of anti-receptor antibodies of hypophyseal thyroid simulation. Case report and estimated incidence]
Autor: S, Pasquier, T, Torresani, E, Werder, H E, Gnehm
Publikováno v: Schweizerische medizinische Wochenschrift. 127(44)
Transient neonatal hypothyroidism induced by transplacental transfer of thyrotropin receptor-blocking antibodies is rare, but should be diagnosed early because its course, treatment, and prognosis are different from the other forms of congenital hypo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a1d9a294063b4a2efa8fd8e9779d2879
https://pubmed.ncbi.nlm.nih.gov/9446201
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6
Neurological and adrenal dysfunction in the adrenal insufficiency/alacrima/achalasia (3A) syndrome
Autor: J H Wales, P J Milla, M Ginalska-Malinowska, Miroslav Dumić, D B Grant, N D Barnes, R J Rowlatt, E Werder, R Steendijk, W von Petrykowski
Publikováno v: Archives of disease in childhood. 68(6)
Review of 20 patients with glucocorticoid deficiency (three cases also with salt loss) associated with absent tear secretion (19 cases) and achalasia of the cardia (15 cases) revealed neurological abnormalities in 17 including hyper-reflexia, muscle
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14cf211ad7ec374a8b5d09f29764efdb
https://pubmed.ncbi.nlm.nih.gov/8333772
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8
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